Tag | Content |
---|
EnhancerAtlas ID | HS042-17893 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr16:69122950-69124350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr16:69123172-69123186 | GAGAGATGAGTCAT | + | 6.43 |
|
| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_34056 | chr16:69122696-69124323 | HCC1954 | SE_68871 | chr16:69122704-69123978 | H9 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH16I069089 | chr16 | 69123051 | 69123810 |
|
Enhancer Sequence | TGTTTCAGCT CCTCTTCTCT GGTAGCAGCA GTTTCTCCTC TTTGGCTCAA AAAGGAGAGC 60 AAGCGTGTTG ATCTACCCTG GGTCCATCCA CCTGTTTTGT CTCTTTGTCT GCGAGGGTGA 120 CTGAATGAAG TGCTGCCTGC CACCTGACTG TGCCTCTCAC CCAACTGTTT GCCGCATTGG 180 AGGGCTGGCT ACAACATGTG AAAGTGGATC AATTGATAAG TCGAGAGATG AGTCATCTGA 240 CCTGTGCAAA ACCAGATAAG CTTCTGCAGT CTTTGCACAG AAATCTAAAA TCTCGGCCAG 300 AATTTCTGTG GCAAAGGGAG AGAGTCAGAA ACCGGAGCTG TGAGAGGTGC CACATTTCCC 360 TGACTATGAG GGGTCTTCTT CCCCAATACG CCCCTTCCCC CAGCAGCAGC TTTGACCTCA 420 GAGGGCCTGG CTGTGTCCTC AGCAAGCTCT GCAGCTACAG ACATGCTGCA GTCACATGCA 480 GCAGCCACAC TGCAGTGCGC GGCACCTCTG CCTGCCATGC TCCACTCTGT TGGAACTGAA 540 TCACCGCTTG GGGGTTGGGA ACCTGTGTTG CTCCTTACAA TACCCGGTGC TGCCTCTTTC 600 CTGCAGGCAG AGCTCAGGGC TGTGCTCAGC GCCCTCTGCA CAGGCTGGCA AGGTGAGAGG 660 GGAATGCAGA CCCCACCTTC GGCCCTGGAA AGCTGAAACA TCATTAGGGA GGTCATCCCC 720 TGTTGTCCTC CCCAGTTCTT CATAGGGAGT CCGTAGCTCC ACGCTACCAG GCCTCAGTTT 780 TTGTGCCCCT CCTCCAGAGT GCCCTCTGCG GTTCTTTGTA ACACAGTGTT GCAAGATCAG 840 TGTTTGCATT TCCTTTATTT TGGAAAGTCA TTTTCCATCC ATAAGCTTGT CTGATTCTCA 900 CAACAATCTT GAAGAACAGG GAGGCAGGCT CTTGACATCC TCCCTTGGTG GGATTTGGCT 960 CCAAGTCTGC TGGGTCGCAG CCAGGAGCCT GTTTACTACA TCGGAAGACC CTCCATGAAA 1020 TGTTTTGAAC ATCTGTTGAA TACAATGGAG CTTCTTCCCA CAAAGTGAGT ACAGAAGTAC 1080 AAGCCTTTCA AGCAGAGTAG AGTTTGAGAT GCAAACTCAG GTACTCACAT ATACACATGA 1140 ATCCCAACAC GTGGGGCCCA CCAAGAAGGC GTTTGTGCTC CACTGACACA TGGTCGGCGC 1200 TGCCTACCAC CTCCCCCGTG CTGGCCCTCT GCCCTCCAGT CTGAGGAGTG GTACAGCCCG 1260 CAGGTACAAT GCCTGGCTGC TGTGCGTATT TGTGTACATT TTCAGATGAT ACGTGATGTG 1320 ACTTAGAACA AGTTTAATGT ATCTGTAGTT TGTAATATGT GCACTTGGCA CTTTTTTTTT 1380 GGAGACAGTC TCTCTCTGTC 1400
|